Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0729264
Disease: Preterm premature rupture of membranes (disorder)
Preterm premature rupture of membranes (disorder) 		2 0 1 0.50 0 0
CUI: C4025186
Disease: T-cell lymphoma/leukemia
T-cell lymphoma/leukemia 		2 0 1 0.50 0 0
CUI: C0264683
Disease: Coronary artery atheroma
Coronary artery atheroma 		6 0 1 0.17 0 0
CUI: C0262428
Disease: Collagen-vascular disease
Collagen-vascular disease 		7 0 1 0.14 0 0
CUI: C0340194
Disease: Respiratory failure without hypercapnia
Respiratory failure without hypercapnia 		9 0 1 0.11 0 0
CUI: C0155164
Disease: Conjunctival scar
Conjunctival scar 		14 0 1 7.1E-02 0 0
CUI: C0020225
Disease: Hydranencephaly
Hydranencephaly 		15 0 1 6.7E-02 0 0
CUI: C1282359
Disease: Ocular Cicatricial Pemphigoid
Ocular Cicatricial Pemphigoid 		15 0 1 6.7E-02 0 0
CUI: C1333964
Disease: Liver Dysplastic Nodule
Liver Dysplastic Nodule 		15 0 1 6.7E-02 0 0
CUI: C2363866
Disease: Traumatic occlusion
Traumatic occlusion 		15 0 1 6.7E-02 0 0
CUI: C0268362
Disease: Osteogenesis imperfecta type III (disorder)
Osteogenesis imperfecta type III (disorder) 		18 0 1 5.6E-02 0 0
CUI: C1848654
Disease: Broad ribs
Broad ribs 		18 0 1 5.6E-02 0 0
CUI: C0030804
Disease: Pemphigoid, Benign Mucous Membrane
Pemphigoid, Benign Mucous Membrane 		19 0 1 5.3E-02 0 0
CUI: C0016049
Disease: Fibromatosis, Gingival
Fibromatosis, Gingival 		20 0 1 5.0E-02 0 0
CUI: C1865244
Disease: Shallow orbits
Shallow orbits 		20 0 1 5.0E-02 0 0
CUI: C0015944
Disease: Fetal Membranes, Premature Rupture
Fetal Membranes, Premature Rupture 		22 0 1 4.5E-02 0 0
CUI: C0262431
Disease: Compression fracture of vertebral column
Compression fracture of vertebral column 		25 0 1 4.0E-02 0 0
CUI: C1290344
Disease: Nonspecific interstitial pneumonia
Nonspecific interstitial pneumonia 		28 0 1 3.6E-02 0 0
CUI: C0079293
Disease: Epidermolysis Bullosa Acquisita
Epidermolysis Bullosa Acquisita 		32 0 1 3.1E-02 0 0
CUI: C0011436
Disease: Dentinogenesis Imperfecta
Dentinogenesis Imperfecta 		35 0 1 2.9E-02 0 0
CUI: C0238281
Disease: Middle Cerebral Artery Syndrome
Middle Cerebral Artery Syndrome 		35 0 1 2.9E-02 0 0
CUI: C0241703
Disease: High pitched voice
High pitched voice 		35 0 1 2.9E-02 0 0
CUI: C0740376
Disease: Middle Cerebral Artery Thrombosis
Middle Cerebral Artery Thrombosis 		35 0 1 2.9E-02 0 0
CUI: C0751845
Disease: Middle Cerebral Artery Embolus
Middle Cerebral Artery Embolus 		35 0 1 2.9E-02 0 0
CUI: C0751846
Disease: Left Middle Cerebral Artery Infarction
Left Middle Cerebral Artery Infarction 		35 0 1 2.9E-02 0 0